Canonical Allele Identifier: CA1012083096
Gene: LINC02775 HGNC NCBI

Linked Data

gnomAD v3: 1-214088007-T-A
gnomAD v4: 1-214088007-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.214088007T>A , CM000663.2:g.214088007T>A GRCh38
NC_000001.10:g.214261350T>A , CM000663.1:g.214261350T>A GRCh37
NC_000001.9:g.212327973T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011510303.1:c.-188-15569A>T XP_011508605.1:n.-188-15569A>T
XR_922584.1:n.119-15569A>T
XR_922584.2:n.261-15569A>T
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